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The protein encoded by ACRBP is similar to proacrosin binding protein sp32 precursor found in mouse, guinea pig, and pig. Additionally we are shipping Acrosin Binding Protein Antibodies (23) and Acrosin Binding Protein Proteins (4) and many more products for this protein.
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ACRBP can be used as a molecular marker for spermatogenesis and sexual maturity in horses.
Down regulation of OY-TES-1 increased expression of apoptosis-regulated protein caspase-3 (show CASP3 ELISA Kits), and decreased expression of cell cycle-regulated protein cyclin E (show CCNE1 ELISA Kits), migration/invasion-regulated proteins MMP2 (show MMP2 ELISA Kits) and MMP9 (show MMP9 ELISA Kits).
OY-TES-1 downregulation in liver cancer cells caused 2 opposite effects on cell proliferation: promotion by upregulating CCND2 (show CCND2 ELISA Kits) and CDCA3, and inhibition by CD9 (show CD9 ELISA Kits) upregulation and NANOG (show NANOG ELISA Kits) downregulation. OY-TES-1 may play multiple roles in liver cancer.
OY-TES-1 was expressed in ovarian cancer (OC) tissues with a high proportion, and some of OC tissues presented OY-TES-1 expression in high level vs OC adjacent tissues.
OY-TES-1 is frequently expressed in colorectal carcinoma and is able to induce humoral immune response spontaneously in CRC (show CALR ELISA Kits) patients.
The down-regulation of OY-TES-1 expression in bone marrow-derived mesenchymal stem cells caused cell growth inhibition, cell cycle arrest, apoptosis induction and migration ability attenuation.
High ACRBP expression correlated with reduced survival time and faster relapse among ovarian cancer patients.
We showed identification of HLA-A24 (show CD164 ELISA Kits)-binding OY-TES-1 peptide, TES (show TES ELISA Kits)(401-409) (KTPFVSPLL) recognized by CD8 (show CD8A ELISA Kits) T-cells.
Data show that sperm protein 32 (sp32) expression was higher and significantly higher in capacitated and post-acrosomal reaction sperms than in frozen-thawed sperms and fresh semen, respectively.
ACRBP-null male mice showed a severely reduced fertility, because of malformation of the acrosome.
Two forms of Acrbp mRNA-wild-type Acrbp-W and variant Acrbp-V5 mRNAs-were generated by alternative splicing of Acrbp in the mouse.
Data suggest that the fertility defect in PCSK4 (proprotein convertase subtilisin/kexin type 4 (show PCSK4 ELISA Kits)) knockout mice is due, in part, to altered processing/proteolysis of ACRBP as well as structural abnormalities in sperm heads and acrosomes.
The protein encoded by this gene is similar to proacrosin binding protein sp32 precursor found in mouse, guinea pig, and pig. This protein is located in the sperm acrosome and is thought to function as a binding protein to proacrosin for packaging and condensation of the acrosin zymogen in the acrosomal matrix. This protein is a member of the cancer/testis family of antigens and it is found to be immunogenic. In normal tissues, this mRNA is expressed only in testis, whereas it is detected in a range of different tumor types such as bladder, breast, lung, liver, and colon.
acrosin binding protein
, proacrosin binding protein sp32
, acrosin-binding protein-like
, acrosin-binding protein
, cancer/testis antigen 23
, cancer/testis antigen OY-TES-1
, proacrosin binding protein
, proacrosin-binding protein sp32
, Acrosin-binding protein
, proacrosin-binding protein (sp32)